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rs63750604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750604(A;A)
Make rs63750604(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position37047577
GeneMLH1
is asnp
is mentioned by
dbSNPrs63750604
ebirs63750604
HLIrs63750604
Exacrs63750604
Varsomers63750604
Maprs63750604
PheGenIrs63750604
hapmaprs63750604
1000 genomesrs63750604
hgdprs63750604
ensemblrs63750604
gopubmedrs63750604
geneviewrs63750604
scholarrs63750604
googlers63750604
pharmgkbrs63750604
gwascentralrs63750604
openSNPrs63750604
23andMers63750604
23andMe allrs63750604
SNP Nexus

SNPshotrs63750604
SNPdbers63750604
MSV3drs63750604
GWAS Ctlgrs63750604
Max Magnitude0
ClinVar
Risk rs63750604(A;A)
Alt rs63750604(A;A)
Reference rs63750604(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37089068G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075365.2,